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AMGEN MANUFACTURING LIMITED

⚠️ Moderate Risk

FEI: 3015532323 • Montrose, PA • UNITED STATES

FEI

FEI Number

3015532323

📍

Location

Montrose, PA

🇺🇸
🏢

Address

16888 State Route 706, , Montrose, PA, United States

Moderate Risk

FDA Import Risk Assessment

38.3
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

1
Total Refusals
2
Unique Violations
8/27/2019
Latest Refusal
8/27/2019
Earliest Refusal

Score Breakdown

Violation Severity
85.0×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
Frequency
10.0×10%
How is this score calculated?

Proprietary Algorithm

  • 40% Violation Severity — AI-assessed (1-10)
  • 30% Refusal Volume — Logarithmic scale
  • 20% Recency — Decays over 5 years
  • 10% Frequency — Refusals per year

© ImportRefusal.com Original Analysis

Violation Summary

271×

DRUG GMPS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the methods used in and controls used for the manufacture, processing, packing, or holding of drugs and other products do not appear to conform to current good manufacturing practices within the meaning of Section 501(a)(2)(B).

751×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

Refusal History

DateProductViolationsDivision
8/27/2019
64OCK02DENOSUMAB, MONOCLONAL ANTIBODIES
27DRUG GMPS
75UNAPPROVED
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is AMGEN MANUFACTURING LIMITED's FDA import refusal history?

AMGEN MANUFACTURING LIMITED (FEI: 3015532323) has 1 FDA import refusal record(s) in our database, spanning from 8/27/2019 to 8/27/2019.

What is an FEI number?

FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. AMGEN MANUFACTURING LIMITED's FEI number is 3015532323.

What types of violations has AMGEN MANUFACTURING LIMITED received?

AMGEN MANUFACTURING LIMITED has been cited for 2 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.

Where does this information about AMGEN MANUFACTURING LIMITED come from?

All FDA import refusal data for AMGEN MANUFACTURING LIMITED is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.

Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.